Canonical Allele Identifier: PA2826998197
Gene: RARS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 215080
ClinVar RCV Id: RCV000727871 RCV000765897
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305714.1:p.Arg83His
CA323244
NM_001318785.2:c.248G>A